Evidence map›Paper›PMID 40063522›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2025

ALDH2 Deficiency and Alcohol Intake in the United States: Opportunity for Precision Cancer Prevention.

Danielle Forman, Manxi Yang, Ryan Chien, Hester Nguyen, Caressa Wong, Jacqueline H J Kim, Argyrios Ziogas, Hannah Lui Park

Abstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Danielle FormanDepartment of Chemistry and Biochemistry, University of California, Los Angeles, California.ORCID 0000-0002-8521-5734
Manxi YangDepartment of Epidemiology and Biostatistics, University of California, Irvine, California.ORCID 0009-0002-5795-5054
Ryan ChienDepartment of Pathology and Laboratory Medicine, University of California, Irvine, California.ORCID 0009-0002-6781-3420
Hester NguyenDepartment of Statistics, University of California, Irvine, California.ORCID 0009-0008-1624-695X
Caressa WongDepartment of Biological Sciences, University of California, Irvine, California.ORCID 0009-0002-8272-8523
Jacqueline H J KimDepartment of Medicine, University of California, Irvine, California.ORCID 0000-0002-4827-3927
Argyrios ZiogasDepartment of Medicine, University of California, Irvine, California.ORCID 0000-0003-4529-3727
Hannah Lui ParkDepartment of Epidemiology and Biostatistics, University of California, Irvine, California.ORCID 0000-0001-9973-1396

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
National Institutes of Health (NIH) P30CA062203NCI NIH HHS P30 CA062203
6 · The paper itself

Abstract

backgroundAlcoholic beverages and the main metabolite of alcohol, acetaldehyde, are known carcinogens. A genetic variant in aldehyde dehydrogenase 2 (ALDH2, G>A, rs671) leads to decreased efficiency in metabolizing acetaldehyde and is associated with an increased cancer risk. As alcohol consumption is a modifiable risk factor for various cancers, the identification of ALDH2 deficiency presents an opportunity for precision cancer prevention.

methodsOur primary objectives were to examine the prevalence of ALDH2 deficiency and alcohol consumption behavior among affected individuals within a large, diverse US national cohort. The prevalence of ALDH2 deficiency was determined by examining the rs671 genotype among 311,290 participants within the All of Us Research Program. Relationships among self-reported alcohol consumption, sociodemographic factors, and the rs671 genotype were analyzed.

resultsALDH2 deficiency was most prevalent among individuals who identified as Asian, among whom 23.5% had at least one deficient ALDH2 allele compared with <2.5% in all other racial/ethnic groups. Among those with one and two deficient ALDH2 alleles, 61.2% and 24.4% reported drinking in the past year, respectively, and of these, 30.3% and 16.0% reported binge drinking. Multivariable analysis showed that ALDH2 genotype, sex, age, race, education, income, employment, marital status, and country of birth were associated with alcohol consumption behavior.

conclusionsMost individuals with ALDH2 deficiency reported drinking alcohol in the past year, and consumption was associated with various sociodemographic variables, particularly sex, age, and country of birth. IMPACT: Our findings suggest a significant opportunity for precision cancer prevention targeting the unique prevalence of ALDH2 deficiency among Asian Americans.

Indexed as

Alcohol DrinkingAldehyde Dehydrogenase, MitochondrialNeoplasmsAdultAgedCohort StudiesFemaleGenotypeHumansMaleMiddle AgedPrecision MedicinePrevalenceRisk FactorsUnited StatesAldehyde Dehydrogenase, MitochondrialALDH2 protein, human

Identifiers

PMID40063522
PMCPMC12048207

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.